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Journal articles on the topic 'Pathology Histology'

Author: Grafiati

Published: 4 June 2021

Last updated: 16 February 2022

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1

Siegel, David A., Reda Wilson, Edward J. Wilkinson, Julia W. Gargano, Meg Watson, Brenda Y. Hernandez, Marc T. Goodman, Charles F. Lynch, Elizabeth R. Unger, and Mona Saraiya. "Evaluation of the Vulvar Cancer Histology Code Reported by Central Cancer Registries: Importance in Epidemiology." Archives of Pathology & Laboratory Medicine 141, no. 1 (October 20, 2016): 139–43. http://dx.doi.org/10.5858/arpa.2015-0422-oa.

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Context.—Knowing the subtype of vulvar cancer histology is important for estimating human papillomavirus–related cancer etiology. Surveillance of human papillomavirus–related vulvar cancers informs public health decisions related to vaccination against human papillomavirus. Objective.—To assess the accuracy of registry classifications of vulvar cancer and determine the histologic classification of cases reported as not otherwise specified. Design.—Pathology specimens were collected from Florida, Iowa, and Hawaii cancer registries. Registry diagnosis was compared with the pathology report from the medical record and a single expert study histology review of a representative histologic section from each case. Results.—The study included 60 invasive vulvar squamous cell carcinoma (SCC) cases, 6 Paget disease cases, 2 basal cell carcinoma cases, and 53 in situ cases. Comparing subtypes of invasive vulvar SCC, the registry agreed with the pathology report classification in 49 of 60 cases (81.7%). Study histology review identified the same SCC subtype as the registry in 9 of 60 cases (15.0%) and the same SCC subtype as the pathology report in 11 of 60 cases (18.3%). Whereas the registry and pathology reports classified 37 and 34 cases, respectively, as being SCC not otherwise specified, the study histology review identified a more specific subtype in all cases. Conclusions.—Subtypes of vulvar cancer were frequently recorded as not otherwise specified in the cancer registry primarily because the pathology report often did not specify the histologic subtype. Vulvar cancer registry data are useful for tracking broad diagnostic categories, but are less reliable for vulvar cancer subtypes.

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2

Rosenbruch, M. "The canine nose—anatomy—histology—pathology." Journal of Veterinary Behavior 4, no. 6 (November 2009): 242. http://dx.doi.org/10.1016/j.jveb.2009.05.011.

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3

Ritchie, A. C., and C. J. Benjamin. "Histology, Histochemistry, and Pathology of Mesothelioma." Journal of Histotechnology 10, no. 4 (December 1987): 269–71. http://dx.doi.org/10.1179/his.1987.10.4.269.

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4

Khavkin, Jeannie, and David A. F. Ellis. "Aging Skin: Histology, Physiology, and Pathology." Facial Plastic Surgery Clinics of North America 19, no. 2 (May 2011): 229–34. http://dx.doi.org/10.1016/j.fsc.2011.04.003.

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5

Claudepierre, Pascal, and Marie-Catherine Voisin. "The entheses: histology, pathology, and pathophysiology." Joint Bone Spine 72, no. 1 (January 2005): 32–37. http://dx.doi.org/10.1016/j.jbspin.2004.02.010.

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6

Christen, Brigitte, W. Wegmann, and P. Vogt. "Clinical Pathology and Histology of Pleural Plaques." Indoor and Built Environment 6, no. 2 (March 1997): 79–85. http://dx.doi.org/10.1177/1420326x9700600205.

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7

Downie, T. "Advanced Laboratory Methods in Histology and Pathology." Histopathology 26, no. 1 (January 1995): 96–97. http://dx.doi.org/10.1111/j.1365-2559.1995.tb00633.x.

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8

Christen, Brigitte, W. Wegmann, and P. Vogt. "Clinical Pathology and Histology of Pleural Plaques." Indoor and Built Environment 6, no. 2 (1997): 79–85. http://dx.doi.org/10.1159/000463309.

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9

Lee, Christine H., Oluyemi Akin-Olugbade, and Alexander Kirschenbaum. "Overview of Prostate Anatomy, Histology, and Pathology." Endocrinology and Metabolism Clinics of North America 40, no. 3 (September 2011): 565–75. http://dx.doi.org/10.1016/j.ecl.2011.05.012.

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10

Li, Guo-Liang, Guy Fontaine, Jine Wu, Shuanliang Fan, Chaofeng Sun, and Ardan M. Saguner. "Atrial dysplasia in the atria of humans without cardiovascular disease." Journal of Investigative Medicine 67, no. 6 (February 14, 2019): 971–76. http://dx.doi.org/10.1136/jim-2018-000916.

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Research on atrial histology of humans without cardiovascular disease is scarce. Therefore, our aim was to study human atrial histology in subjects without cardiovascular disease. Histology of the right atrium, left atrium or atrial septum was studied in eight patients (one newborn infant and seven adults) who died of a non-cardiac cause and who were not known to suffer from any cardiovascular pathology. Staining with hematoxylin phloxine saffron or Masson’s trichrome was performed to have a better identification of fibrosis and H&E for better identification of lymphocytes. Atrial histology was compared with the histology of the left ventricle and was taken from a collection of standard glass slides. Common light microscopic examination and numeric image processing was performed in all samples. Left atrial histology showed a substantial amount of adipocytes and interstitial fibrosis, associated with replacement fibrosis in some of these cases including one case of lymphocytic infiltrates, similar to the histologic changes of the right ventricle (RV) known in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVD). Furthermore, we identified a perpendicular orientation of atrial myocardial fibres, which is also a feature of the thin RV free wall. A similar histologic substrate to the RV myocardium known in ARVD is found in the atria of humans without an overt cardiovascular pathology. This may explain the high prevalence of atrial fibrillation in the general population.

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11

El Achi, Hanadi El, and Joseph D. Khoury. "Artificial Intelligence and Digital Microscopy Applications in Diagnostic Hematopathology." Cancers 12, no. 4 (March 26, 2020): 797. http://dx.doi.org/10.3390/cancers12040797.

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Digital Pathology is the process of converting histology glass slides to digital images using sophisticated computerized technology to facilitate acquisition, evaluation, storage, and portability of histologic information. By its nature, digitization of analog histology data renders it amenable to analysis using deep learning/artificial intelligence (DL/AI) techniques. The application of DL/AI to digital pathology data holds promise, even if the scope of use cases and regulatory framework for deploying such applications in the clinical environment remains in the early stages. Recent studies using whole-slide images and DL/AI to detect histologic abnormalities in general and cancer in particular have shown encouraging results. In this review, we focus on these emerging technologies intended for use in diagnostic hematology and the evaluation of lymphoproliferative diseases.

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12

Rose, P. G., F. R. Reale, M. L. Beurskens, and R. E. Hunter. "Preoperative CA-125 levels predict poor prognostic pathologic features in early stage, FIGO grade 1 and 2 endometrial adenocarcinoma." International Journal of Gynecologic Cancer 3, no. 4 (1993): 259–63. http://dx.doi.org/10.1046/j.1525-1438.1993.03040259.x.

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Preoperative CA-125 levels were studied in patients with favorable histology and early clinical stage endometrial adenocarcinoma to determine its ability to predict the presence of poor pathologic prognostic features on final pathology. One hundred and one patients with clinical stage I (N= 65) or II (N= 19) or diagnosed by endometrial curettage (EMC) only (N-17) with grade 1 or 2 endometrial adenocarcinoma without gross cervical involvement underwent preoperative CA-125 levels. Final pathology was reviewed for five poor prognostic pathologic features: FIGO grade 3 histology, unfavorable histologic type (sarcoma, clear cell, or papillary serous), invasion into the outer third of the myometrium, extension to the cervix, and extra-uterine metastases. Fifteen patients (14.9%) had CA-125 levels greater than 30 IU ml−1. Of these 15 patients, 12 had one or more of the five poor prognostic pathologic features (positive predictive value 80.0%, specificity 95.8%,P< 0.0001). However, since 30 of the 101 patients were found to have one or more of these poor prognostic pathologic features the sensitivity was only 40.0%. When clinical stage I patients were analyzed separately three patients (4.6%) had CA-125 levels greater than 30 IU ml −1 (positive predictive value 100%, specificity of 100%, sensitivity of 21.4%,P= 0.008). For patients with clinical stage II carcinoma, CA-125 was not predictive of pathologic findings except as a negative predictor of disease in a subgroup of patients whose endocervical curettage (ECC) demonstrated carcinoma unattached to endocervical tissue. In patients diagnosed by EMC only, an elevated CA-125 level was associated with poor prognostic pathologic features (P= 0.001). An elevated preoperative CA-125 reliably predicts advanced disease even in patients with apparently favorable histology and clinical stage, however the sensitivity of this method remains low.

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13

Langer, Corey J., Benjamin Besse, Antonio Gualberto, Elizabeth Brambilla, and Jean-Charles Soria. "The Evolving Role of Histology in the Management of Advanced Non–Small-Cell Lung Cancer." Journal of Clinical Oncology 28, no. 36 (December 20, 2010): 5311–20. http://dx.doi.org/10.1200/jco.2010.28.8126.

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Until recently, non–small-cell lung cancer (NSCLC) was treated as a single disease despite recognition of its histologic and molecular heterogeneity. Recent clinical trials, however, demonstrate that histology is an important factor for individualizing treatment, based on either safety or efficacy outcomes. For example, the labeling of the licensed agents bevacizumab and pemetrexed is restricted to patients with nonsquamous cell NSCLC. For bevacizumab, this restriction is due to an apparent association between squamous cell histology and severe pulmonary hemorrhage, whereas for pemetrexed, superior treatment effects have been observed in patients with nonsquamous cell histology. Given fewer agents are both active and tolerable in patients with squamous cell carcinoma compared with adenocarcinoma, and the nature of this particular phenotype of NSCLC, new drugs are needed for this histology. In this new histology-based treatment era, questions persist. Can pathology accurately distinguish the histologic subtypes of NSCLC? Can we use cytologic diagnosis? In the future, will molecular profiling of tumors trump histologic analysis? Herein we describe how therapy for NSCLC is evolving on the basis of a better understanding of molecular mechanisms underlying NSCLC histologic heterogeneity and tumorigenesis.

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14

Cotton, D. W. K., and T. J. Stephenson. "Autopsy histology." Journal of Pathology 154, no. 4 (April 1988): 299–300. http://dx.doi.org/10.1002/path.1711540404.

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15

Condel, Jennifer L., Drazen M. Jukic, David T. Sharbaugh, and Stephen S. Raab. "Histology Errors." Pathology Case Reviews 10, no. 2 (March 2005): 82–87. http://dx.doi.org/10.1097/01.pcr.0000155793.51378.ba.

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16

ROBERTS, SALLY, HELENA EVANS, JAYESH TRIVEDI, and JANIS MENAGE. "HISTOLOGY AND PATHOLOGY OF THE HUMAN INTERVERTEBRAL DISC." Journal of Bone and Joint Surgery-American Volume 88 (April 2006): 10–14. http://dx.doi.org/10.2106/00004623-200604002-00003.

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17

Roberts, Sally. "Histology and Pathology of the Human Intervertebral Disc." Journal of Bone and Joint Surgery (American) 88, suppl_2 (April 1, 2006): 10. http://dx.doi.org/10.2106/jbjs.f.00019.

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18

Danguy, A., K. Kayser, N. V. Bovin, and H. J. Gabius. "The Relevance of Neoglycoconjugates for Histology and Pathology." Trends in Glycoscience and Glycotechnology 7, no. 36 (1995): 261–75. http://dx.doi.org/10.4052/tigg.7.261.

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19

Lazar, T. "Histology and Cell Biology—An Introduction to Pathology." Tissue and Cell 34, no. 6 (December 2002): 460. http://dx.doi.org/10.1016/s0040816602000733.

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20

Woods, Yvonne L., and Frank A. Carey. "Pathology and histology of the oesophagus and stomach." Surgery (Oxford) 32, no. 11 (November 2014): 575–80. http://dx.doi.org/10.1016/j.mpsur.2014.09.004.

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21

Woods, Yvonne L., and Frank A. Carey. "Pathology and histology of the oesophagus and stomach." Surgery (Oxford) 35, no. 11 (November 2017): 612–18. http://dx.doi.org/10.1016/j.mpsur.2017.08.002.

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22

Stelow, Edward B. "“Normal Histology” in Diagnostic Pathology Series By Amirsys." American Journal of Surgical Pathology 38, no. 5 (May 2014): 728. http://dx.doi.org/10.1097/pas.0000000000000196.

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23

Pfister, Stefan, Christian Hartmann, and Andrey Korshunov. "Histology and Molecular Pathology of Pediatric Brain Tumors." Journal of Child Neurology 24, no. 11 (October 19, 2009): 1375–86. http://dx.doi.org/10.1177/0883073809339213.

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24

WELLS, M., and J. N. BULMER. "The human placental bed: histology, immunohistochemistry and pathology." Histopathology 13, no. 5 (April 3, 2007): 483–98. http://dx.doi.org/10.1111/j.1365-2559.1988.tb02073.x.

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25

Odze, Robert D. "Barrett esophagus: histology and pathology for the clinician." Nature Reviews Gastroenterology & Hepatology 6, no. 8 (July 7, 2009): 478–90. http://dx.doi.org/10.1038/nrgastro.2009.103.

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26

Müllauer, Leonhard. "Milestones in pathology—from histology to molecular biology." memo - Magazine of European Medical Oncology 10, no. 1 (January 9, 2017): 42–45. http://dx.doi.org/10.1007/s12254-016-0307-z.

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27

Dash, Rajesh C. "Histology and Cell Biology: An Introduction to Pathology." Archives of Pathology & Laboratory Medicine 127, no. 7 (July 1, 2003): 896–97. http://dx.doi.org/10.5858/2003-127-896-hacbai.

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28

Wold, Lester E. "Practical Approach to Processing Osteosarcomas in the Surgical Pathology Laboratory." Pediatric and Developmental Pathology 1, no. 5 (September 1998): 449–54. http://dx.doi.org/10.1007/s100249900062.

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The pathologic assessment of definitive surgical specimens in patients treated for osteosarcoma can be rapidly accomplished using a few pieces of special equipment. Rapid decalcification with formic acid–formalin and routine tissue processing allow the histology laboratory to rapidly prepare histologic slides for pathologic evaluation. A simple qualitative assessment of tumor response to chemotherapy allows the pathologist to classify the tumor response rapidly and reproducibly, and a simple report format allows for unambiguous communication with the patient and physician.

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29

Kumar, Kiran, Kaveri Hallikeri, and Veda Hegde. "Evaluation of Use of Digital Method In Studying Histology and Pathology among Undergraduate Students of Dentistry." Indian Journal of Dental Education 12, no. 1 (2019): 5–10. http://dx.doi.org/10.21088/ijde.0974.6099.12119.1.

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30

Gruber-Mösenbacher, Ulrike, Lauren Katzell, Mark McNeely, Elisabeth Neier, Bobo Jean, Avelino Kuran, and Srikar Chamala. "Digital Pathology in Cameroon." JCO Global Oncology, no. 7 (August 2021): 1380–89. http://dx.doi.org/10.1200/go.21.00166.

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PURPOSE Cancer is becoming increasingly prevalent among the group of treatable diseases in African countries. There is a shortage of clinicians and pathologists available for cancer diagnosis and treatment. These limited resources must be efficiently used to maximize the number of patients treated. One of the critical factors in treatment efficiency is the correct and timely diagnosis of specimens by pathologists. However, there is currently a significant shortage of cancer care clinicians in Africa and an even more considerable shortage of pathologists. This article presents an example in which telepathology was used to mitigate the lack of pathologists in Cameroon. METHODS The telepathology workaround was implemented in a district hospital based in Cameroon's Adamawa region, where a European surgeon provides cancer treatment. A small histology laboratory there is run by one histotechnologist who processes surgical biopsies into histology slides. As there are no pathologists on site, these slides are digitally scanned using a mobile phone and a whole slide imaging (WSI) scanner. The slides are then shared electronically with a volunteering pathologist in Europe who provides a diagnostic report. RESULTS From 2018 to July 2019, specimens for 101 patients were photographed through an iPhone connected to a microscope eyepiece producing several individual images per specimen. From July 2019 to December 2020, slides from 282 patients were scanned using WSI and digitally transmitted. CONCLUSION WSI on hematoxylin and eosin histology slides for remote diagnosis can increase cancer treatment efficacy and reduce overtreatment of tumors clinically suspicious for malignancy in under-resourced countries with a lack of pathologists.

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31

Ireland, Karen. "Histology for pathologists." Human Pathology 23, no. 10 (October 1992): 1195. http://dx.doi.org/10.1016/0046-8177(92)90044-4.

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32

Taylor, Glenn P. "Pathology of the Pediatric Regio Inguinalis: Mysteries of the Hernia Sac Exposed." Pediatric and Developmental Pathology 3, no. 6 (November 2000): 513–24. http://dx.doi.org/10.1007/s100240010118.

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Inguinal hernia repair is one of the most common surgeries performed on children. However, the value of routine histologic examination of hernia sac tissues continues to be debated. Although the surgical pathology of herniorrhaphy tissues is usually simple, occasional examples have unexpected findings that potentially lead to inappropriate management or that have added clinical implications. These along with surgical-quality assurance issues need to be considered in cost-benefit arguments. This article reviews basic histology, common potential pitfalls, and significant unexpected conditions encountered in the surgical pathology of the inguinal hernia sac in children.

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33

Wilkins, B. S. "Histology of normal haemopoiesis: bone marrow histology. I." Journal of Clinical Pathology 45, no. 8 (August 1, 1992): 645–49. http://dx.doi.org/10.1136/jcp.45.8.645.

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34

Kirchberger, Michael C., Frank Unglaub, Marion Mühldorfer-Fodor, Thomas Pillukat, Peter Hahn, Lars P. Müller, and Christian K. Spies. "Update TFCC: histology and pathology, classification, examination and diagnostics." Archives of Orthopaedic and Trauma Surgery 135, no. 3 (January 10, 2015): 427–37. http://dx.doi.org/10.1007/s00402-015-2153-6.

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35

Danguy, A., C. Decaestecker, F. Genten, I. Salmon, and R. Kiss. "Applications of Lectins and Neoglycoconjugates in Histology and Pathology." Cells Tissues Organs 161, no. 1-4 (1998): 206–18. http://dx.doi.org/10.1159/000046459.

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36

Gilbertson, John, and Yukako Yagi. "Histology, imaging and new diagnostic work-flows in pathology." Diagnostic Pathology 3, Suppl 1 (2008): S14. http://dx.doi.org/10.1186/1746-1596-3-s1-s14.

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37

Coleman, Raymond. "Can histology and pathology be taught without microscopes? The advantages and disadvantages of virtual histology." Acta Histochemica 111, no. 1 (January 2009): 1–4. http://dx.doi.org/10.1016/j.acthis.2008.09.003.

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38

Syed, Sana, and Ryan W. Stidham. "Potential for Standardization and Automation for Pathology and Endoscopy in Inflammatory Bowel Disease." Inflammatory Bowel Diseases 26, no. 10 (September 1, 2020): 1490–97. http://dx.doi.org/10.1093/ibd/izaa211.

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Abstract Automated image analysis methods have shown potential for replicating expert interpretation of histology and endoscopy images, which traditionally require highly specialized and experienced reviewers. Inflammatory bowel disease (IBD) diagnosis, severity assessment, and treatment decision-making require multimodal expert data interpretation and integration, which could be significantly aided by applications of machine learning analyses. This review introduces fundamental concepts of machine learning for imaging analysis and highlights research and development of automated histology and endoscopy interpretation in IBD. Proof-of-concept studies strongly suggest that histologic and endoscopic images can be interpreted with similar accuracy as knowledge experts. Encouraging results support the potential of automating existing disease activity scoring instruments with high reproducibility, speed, and accessibility, therefore improving the standardization of IBD assessment. Though challenges surrounding ground truth definitions, technical barriers, and the need for extensive multicenter evaluation must be resolved before clinical implementation, automated image analysis is likely to both improve access to standardized IBD assessment and advance the fundamental concepts of how disease is measured.

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39

Allen, Timothy Craig. "Pathology of Small Airways Disease." Archives of Pathology & Laboratory Medicine 134, no. 5 (May 1, 2010): 702–18. http://dx.doi.org/10.5858/134.5.702.

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Abstract Context.—The term small airways disease encompasses a generally poorly understood group of lung diseases that may arise primarily within the small airways or secondarily from diseases primarily affecting the bronchi or lung parenchyma. Their histology may be confusing; however, because treatments and prognoses vary, correct pathologic diagnosis is important. Objective.—To present a nonexhaustive review of the pathology of primary and secondary small airways diseases, including small airways disease related to tobacco; to various other exposures, including mineral dusts; to diseases involving other areas of the lung with secondary bronchiolar involvement; and to recently described bronchiolitic disorders. Data sources.—Current literature is reviewed. Conclusions.—Small airways diseases include a wide variety of diseases of which the pathologist must consider. Uncommon conditions such as diffuse idiopathic neuroendocrine cell hyperplasia and diffuse panbronchiolitis may show relatively specific diagnostic features histologically; however, most small airways diseases exhibit nonspecific histologic features. Conditions not considered primary pulmonary diseases, such as collagen vascular diseases, bone marrow transplantation, and inflammatory bowel disease, must also be considered in patients with small airways changes histologically. Clinical and radiologic correlation is important for obtaining the best possible diagnosis.

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40

Upadhyaya, P., C. S. Agarwal, A. K. Karak, S. Karki, A. Pradhan, and T. N. Subba. "Prevalence of Histologically Proven Acute Appendicitis And Incidental Carcinoid Tumour in the Practice of Surgical Pathology at BPKIHS." Health Renaissance 12, no. 3 (July 25, 2016): 197–203. http://dx.doi.org/10.3126/hren.v12i3.15321.

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Background: Appendicitis is the most common cause of acute abdominal pain requiring surgical intervention. Objective: To determine the relative prevalence of histologically proven acute appendicitis in surgically respected specimens with clinical diagnosis of acute appendicitis and also to find out the rate of occurrence of characinoid tumour as an incidental histologic finding.Methods: It is a retrospective study involving all gross specimens received in the department of pathology over a period of twenty months (1.1.2006 to 31.8.2007). Histologic data on 515 appendicectomy samples (clinically diagnosed as appendicitis) of the total 7295 specimens received over a period of twenty months were retrieved from the archives of department of pathology, with exclusion of appendectomy incidental to another surgical procedure.Results: Appendectomy specimens constituted 7.0% (n=515; M:F 1.1:1) of all surgical pathologic specimens (n=7295) at B.P.K.I.H.S. The breakups of histologic diagnoses are: acute appendicitis with or without periappendicitis and gangrenous change (93.6%, n=482), “receding appendicitis” (5.4%, n=28), and normal histology (1.0%, n= 5). Carcinoid tumours were detected incidentally in three cases (0.58%) out of all appendectomy specimens.Conclusion: Analysis of data revealed a prevalence of 6.99% of histologically proven acute appendicitis in this tertiary health care set up. The rate of occurrence of carcinoid tumour was 0.58%.Health Renaissance 2014;12(3): 197-203

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41

Fleming, S. "Basic Histology." Histopathology 16, no. 5 (April 3, 2007): 511. http://dx.doi.org/10.1111/j.1365-2559.1990.tb01556.x.

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42

Hoda, Syed A., and Rana S. Hoda. "Histology for Pathologists." Advances in Anatomic Pathology 15, no. 2 (March 2008): 124. http://dx.doi.org/10.1097/pap.0b013e318166130a.

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43

Lagana, Stephen M., Anil V. Parwani, and Larry C. Nichols. "Cardiac Sarcoidosis: A Pathology-Focused Review." Archives of Pathology & Laboratory Medicine 134, no. 7 (July 1, 2010): 1039–46. http://dx.doi.org/10.5858/2009-0274-ra.1.

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Abstract Context.—Sarcoidosis is a granulomatous disease of unclear etiology. It is not commonly fatal, but when sarcoidosis is fatal, it is most often from cardiac involvement and when sarcoidosis involves the heart, it frequently causes death. The disease presents diagnostic challenges both clinically and histologically. Objectives.—To review the histology of cardiac sarcoidosis and the histologic differential diagnosis of cardiac granulomatous disease and to review the epidemiology and gross pathology of cardiac sarcoid as well as discuss current controversies, clinical diagnostic criteria, and proposed mechanisms of pathogenesis. Data Sources.—We reviewed the literature searchable on PubMed as well as selected older studies revealed by our review of the recent literature. Photographs were taken from cases on file at the University of Pittsburgh Medical Center (Pittsburgh, Pennsylvania) and Columbia University Medical Center (New York, New York). Conclusions.—Sarcoidosis is a focal or disseminated granulomatous disease that likely represents the final common pathway of various pathogenic insults in a genetically susceptible host. The type of insult may influence the specific sarcoid phenotype. Controversy still abounds, but many areas of investigation around sarcoidosis are yielding exciting discoveries and bringing us closer to a richer understanding of this puzzling disease.

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44

Noujaim, Jonathan, Khin Thway, Amna Sheri, Charles Keller, and Robin L. Jones. "Histology-Driven Therapy." International Journal of Surgical Pathology 24, no. 1 (September 22, 2015): 5–15. http://dx.doi.org/10.1177/1066896915606971.

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45

Cree, I. "Histology Picture Tests." Journal of Clinical Pathology 46, no. 5 (May 1, 1993): 486. http://dx.doi.org/10.1136/jcp.46.5.486-a.

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46

Knowles, Daniel M. "Histology for Pathologists." American Journal of Surgical Pathology 16, no. 12 (December 1992): 1249. http://dx.doi.org/10.1097/00000478-199212000-00013.

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47

Renshaw, Andrew A., and Christopher L. Corless. "Histology and Immunohistochemistry." American Journal of Surgical Pathology 19, no. 7 (July 1995): 842–49. http://dx.doi.org/10.1097/00000478-199507000-00013.

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48

Linden, Michael D. "Histology for Pathologists." American Journal of Surgical Pathology 32, no. 7 (July 2008): 1109–10. http://dx.doi.org/10.1097/pas.0b013e3181659143.

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49

Wheeler, James E. "Histology for Pathologists." American Journal of Surgical Pathology 23, no. 9 (September 1999): 1154. http://dx.doi.org/10.1097/00000478-199909000-00022.

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50

Buesa, René J. "Salaries in histology." Annals of Diagnostic Pathology 12, no. 2 (April 2008): 122–27. http://dx.doi.org/10.1016/j.anndiagpath.2007.09.003.

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